A child with a rare genetic disease that affects mitochondria is the first person to receive a new experimental treatment for ...

As West Virginia records the largest reduction in fatal overdoses across the nation over a 12-month period, substance use ...

The value of a recent biochemical discovery can be seen in the case of an 8-year-old boy who was playing typical sports in ...

Microglia replacement therapy helps treat people with a rare genetic condition called ALSP, suggesting the approach could ...

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a progressive neurological disease with an ...

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) is a progressive neurological disease with an ...

An 8-year-old boy, wheelchair-bound due to a rare genetic disease, HPDL deficiency, regained his mobility through an ...

Hudson Institute's leadership in RNA research has again been recognised, this time with a significant research grant from the Victorian government.Dr ...

For those who haven’t entered the valley of middle age, a CAC is a specialized CT scan that looks for calcium deposits in the ...

The World Heath Organisation has warned people of a 'fatal disease' being spread by mosquitoes in two neighbourhoods in Spain ...

Among members of the Richardson family who carry a mutation in the PSEN1 gene, the average age when symptoms start is 39.